NDC 70908-040 Mefactory Pig Collagen 1step Piggy Nose Pack

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70908-040
Proprietary Name:
Mefactory Pig Collagen 1step Piggy Nose Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mefactory Co., Ltd.
Labeler Code:
70908
Start Marketing Date: [9]
12-01-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70908-040-02

Package Description: 10 POUCH in 1 CARTON / .2 g in 1 POUCH (70908-040-01)

Product Details

What is NDC 70908-040?

The NDC code 70908-040 is assigned by the FDA to the product Mefactory Pig Collagen 1step Piggy Nose Pack which is product labeled by Mefactory Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70908-040-02 10 pouch in 1 carton / .2 g in 1 pouch (70908-040-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Mefactory Pig Collagen 1step Piggy Nose Pack?

Indications and usage: Apply sufficient amount of water on your nose. Remove the clear protection film with dry hands. Attach the white strip on the nose and wait for 10-15 minutes until the sheet is completely dry. Remove the dry strip slowly from edge.

Which are Mefactory Pig Collagen 1step Piggy Nose Pack UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Mefactory Pig Collagen 1step Piggy Nose Pack Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".